eprintid: 10105303 rev_number: 8 eprint_status: archive userid: 695 dir: disk0/10/10/53/03 datestamp: 2020-07-15 23:09:13 lastmod: 2020-07-15 23:09:13 status_changed: 2020-07-15 23:09:13 type: thesis metadata_visibility: show creators_name: Venthoye, Maria Geraldine title: Characterisation of an amorphous dry powder aerosol system ispublished: unpub keywords: Health and environmental sciences; Aerosol; Amorphous; Dry; Powder note: Thesis digitised by ProQuest. abstract: Amorphous spray dried powders of "respirable" size have been produced and their potential for use in powder aerosol formulations investigated. The drying conditions for salbutamol sulphate, a hydrophilic respiratory drug, were optimised using the Mini Büchi 190 spray dryer. The feed solution temperature and the location of the yield was found to influence the size and moisture content of the particles. The surface area and morphology were determined for the spray dried samples with comparisons made to micronised particles. The amorphous form is physically and thermodynamically unstable and under favourable temperature and relative humidity will revert back to the stable crystalline species. Various techniques were used to study this conversion and the appropriateness of further processing to induce aggregation. Microcalorimetry revealed; how different drying conditions would affect relative physical stability, the degree of batch to batch variation, and the influence of different carrier lactose types. Increased physical stability was imparted by the addition of amorphous spray dried lactose. In addition, the depression of glass transition temperature with moisture uptake was observed and the production of a partially crystalline form was detected. Aerosol deposition studies were carried out at 60.0 Lmin⁻¹ with the Rotahaler® (Glaxo) using; the Andersen cascade impactor, multistage liquid and twin impingers. Deagglomeration and aerosolisation efficiency was inferred from device retention and oropharyngeal deposition. Respirable mass and fine particle dose indicated the likely degree of deep lung penetration. The impaction methods differed in the amount and reproducibility of the particle size information provided. Significant differences were detected in micronised samples but not in spray dried batches. At 28.3 Lmin⁻¹ the Andersen was unable to adequately disperse and aerosolise the cohesive powders. Size enlargement into aggregates was achieved by tumbling carrier-free and drug/lactose mixes. The size fraction of carrier and the pre-storage humidity of drug significantly affected the measured aerosol properties. date: 1997 oa_status: green full_text_type: other thesis_class: doctoral_open thesis_award: Ph.D language: eng thesis_view: UCL_Thesis primo: open primo_central: open_green verified: verified_manual full_text_status: public pages: 256 institution: UCL (University College London) department: Pharmaceutics thesis_type: Doctoral citation: Venthoye, Maria Geraldine; (1997) Characterisation of an amorphous dry powder aerosol system. Doctoral thesis (Ph.D), UCL (University College London). Green open access document_url: https://discovery.ucl.ac.uk/id/eprint/10105303/1/Characterisation_of_an_amorpho.pdf